EP4191762A1 - Adhesive for battery, and adhesive layered body for battery - Google Patents

Adhesive for battery, and adhesive layered body for battery Download PDF

Info

Publication number
EP4191762A1
EP4191762A1 EP21849441.7A EP21849441A EP4191762A1 EP 4191762 A1 EP4191762 A1 EP 4191762A1 EP 21849441 A EP21849441 A EP 21849441A EP 4191762 A1 EP4191762 A1 EP 4191762A1
Authority
EP
European Patent Office
Prior art keywords
battery
adhesive agent
adhesive
weight
meth
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP21849441.7A
Other languages
German (de)
English (en)
French (fr)
Inventor
Kouichirou Maeda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zeon Corp
Original Assignee
Zeon Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zeon Corp filed Critical Zeon Corp
Publication of EP4191762A1 publication Critical patent/EP4191762A1/en
Pending legal-status Critical Current

Links

Images

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621—Binders
    • H01M4/622—Binders being polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38—Pressure-sensitive adhesives [PSA]
    • C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/385—Acrylic polymers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0561—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of inorganic materials only
    • H01M10/0562—Solid materials
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/10—Metal compounds
    • C08K3/105—Compounds containing metals of Groups 1 to 3 or of Groups 11 to 13 of the Periodic Table
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/04—Non-macromolecular additives inorganic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/06—Non-macromolecular additives organic
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J125/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Adhesives based on derivatives of such polymers
    • C09J125/02—Homopolymers or copolymers of hydrocarbons
    • C09J125/04—Homopolymers or copolymers of styrene
    • C09J125/08—Copolymers of styrene
    • C09J125/10—Copolymers of styrene with conjugated dienes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38—Pressure-sensitive adhesives [PSA]
    • C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/383—Natural or synthetic rubber
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/058—Construction or manufacture
    • H01M10/0585—Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/52—Removing gases inside the secondary cell, e.g. by absorption
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/183—Sealing members
    • H01M50/19—Sealing members characterised by the material
    • H01M50/195—Composite material consisting of a mixture of organic and inorganic materials
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/10—Primary casings; Jackets or wrappings
    • H01M50/183—Sealing members
    • H01M50/19—Sealing members characterised by the material
    • H01M50/197—Sealing members characterised by the material having a layered structure
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
    • C09J2203/33—Applications of adhesives in processes or use of adhesives in the form of films or foils for batteries or fuel cells
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/408—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the adhesive layer
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00—Additional features of adhesives in the form of films or foils
    • C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
    • C09J2301/414—Additional features of adhesives in the form of films or foils characterized by the presence of essential components presence of a copolymer
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2425/00—Presence of styrenic polymer
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2433/00—Presence of (meth)acrylic polymer
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00—Electrolytes
    • H01M2300/0017—Non-aqueous electrolytes
    • H01M2300/0065—Solid electrolytes
    • H01M2300/0068—Solid electrolytes inorganic
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present invention relates to an adhesive agent for battery and an adhesive layered body for battery.
  • an adhesive agent or an adhesive tape may be used for, e.g., effecting adhesion and fixation of battery constituent members to the outer casing of the secondary battery, or for effecting adhesion of the battery constituent members to make those members in a compact state to be stored in the outer casing (Patent literatures 1 and 2).
  • lithium-ion secondary batteries have been put into practical use.
  • the secondary battery with higher reliability and higher energy density.
  • an all-solid-state secondary battery in which a solid electrolyte is adopted as an electrolyte in place of a prior-art solution-based electrolyte is attracting attention.
  • a battery using a sulfide-based solid electrolyte as the solid electrolyte has been developed.
  • the term "sulfide-based solid electrolyte" described herein means a solid electrolyte containing a sulfide.
  • hydrogen sulfide may also be generated when electricity is charged and discharged to the battery containing the sulfide-based solid electrolyte.
  • the hydrogen sulfide When hydrogen sulfide is generated inside the battery, the hydrogen sulfide may corrode a metal current collector that constitutes the battery, resulting in an increase in the resistance value of the metal current collector. Furthermore, in some cases, a gap is generated between the electrodes or the outer casing swells. Thus, hydrogen sulfide inside the battery can be a factor which deteriorates battery performance.
  • the present inventors have conducted intensive studies and, as a result, found that, by adding a metal compound in an amount within a specific range to an adhesive agent used in a battery, the adhesive agent can absorb hydrogen sulfide while exhibiting good adhesive strength, thereby completing the present invention.
  • the present invention provides the following.
  • an adhesive agent for battery that can absorb hydrogen sulfide generated inside the battery containing a sulfide-based solid electrolyte while exhibiting good adhesive strength
  • an adhesive layered body for battery that can absorb hydrogen sulfide generated inside the battery containing a sulfide-based solid electrolyte while exhibiting good adhesive strength to an adherend.
  • Fig. 1 is a schematic cross-sectional view of an adhesive layered body for battery according to an embodiment of the present invention.
  • an “agent” may be composed of one type of substance or may be composed of two or more types of substances.
  • a "resin” may be composed of one type of polymer or may be composed of two or more types of polymers.
  • an “adhesive agent” also includes a tackiness agent (pressure sensitive adhesive agent), unless otherwise specified.
  • (meth)acryl encompasses “acryl” (acrylic, acryl), “methacryl” (methacrylic, methacryl), and combinations thereof.
  • (meth)acrylic acid encompasses “acrylic acid”, “methacrylic acid”, and combinations thereof
  • (meth)acrylamide encompasses "acrylamide", “methacrylamide”, and combinations thereof.
  • (meth)acrylate encompasses “acrylate”, “methacrylate”, and combinations thereof.
  • (meth)acrylo encompasses “acrylo", “methacrylo” and combinations thereof.
  • An adhesive agent for battery according to an embodiment of the present invention includes a metal compound and a resin.
  • the "adhesive agent for battery” may be simply referred to as “adhesive agent”.
  • the adhesive agent for battery according to the present embodiment has hydrogen sulfide absorption ability and good adhesive strength.
  • the resin is composed of a polymer.
  • adhesive properties of the adhesive agent are provided.
  • any optional polymer that is capable of providing the adhesive properties to the adhesive agent may be used.
  • the polymer capable of providing the adhesive properties to the adhesive agent is also called a base polymer.
  • the polymer constituting the resin may include (1) an acrylic polymer and (2) a rubber polymer.
  • the polymer constituting the resin one type of the polymer may be solely used, and two or more types of the polymers may also be used in combination at any ratio.
  • the acrylic polymer means a polymer containing an acrylic compound unit.
  • the acrylic compound unit means a structural unit having a structure obtained by polymerizing an acrylic compound as a monomer.
  • the acrylic compound unit is not limited by production methods thereof, and may be a structural unit obtained by any optional production method.
  • the acrylic compound means (meth)acrylic acid and derivatives thereof.
  • the derivatives of (meth)acrylic acid may include a (meth)acrylic acid ester, a (meth)acrylic anhydride, a (meth)acrylic acid amide, and a (meth)acrylonitrile.
  • Examples of the (meth)acrylic acid esters may include: an ester of (meth)acrylic acid and an alkyl of 1 to 20 carbon atoms (for example, methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl(meth)acrylate, sec-butyl(meth)acrylate, tert-butyl (meth)acrylate, pentyl (meth)acrylate, isopentyl (meth)acrylate, hexyl (meth)acrylate, heptyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, n-octyl (meth)acrylate, isooctyl (meth)acrylate, n-nonyl (meth)acrylate, isononyl (meth)acrylate
  • Examples of the (meth)acrylamides may include (meth)acrylamide, N,N-dimethyl(meth)acrylamide, N,N-diethyl(meth)acrylamide, N,N-dimethylaminopropyl(meth)acrylamide, N-butyl(meth)acrylamide, N-methylol(meth)acrylamide, N-(2-hydroxypropyl)(meth)acrylamide, N-(methoxymethyl)(meth)acrylamide, N-(butoxymethyl)(meth)acrylamide, and diacetone (meth)acrylamide.
  • acrylic compound unit contained in the acrylic polymer one type thereof may be solely used, and two or more types thereof may also be used in combination at any ratio.
  • the acrylic polymer is preferably a polymer containing a (meth)acrylic acid alkyl ester unit.
  • the number of carbon atoms of the alkyl group in the (meth)acrylic acid alkyl ester unit is preferably 1 to 20, more preferably 1 to 10, and still more preferably 1 to 5.
  • the weight ratio of the (meth)acrylic acid alkyl ester unit relative to the total weight of the acrylic compound unit in the acrylic polymer is preferably 80% by weight or more, more preferably 90% by weight or more, and still more preferably 95% by weight or more, and is usually 100% by weight or less, and may be 100% by weight.
  • the acrylic polymer may include an optional monomer unit in addition to the acrylic compound unit.
  • the weight ratio of the acrylic compound unit in all the structural units of the acrylic polymer is preferably 50% by weight or more, more preferably 60% by weight or more, still more preferably 80% by weight or more, and particularly preferably 90% by weight or more, and is usually 100% by weight or less, and may be 100% by weight.
  • Examples of the optional monomer units that may be included in the acrylic polymer may include a vinyl ester unit; a vinyl ether unit; an olefin unit; a substituted olefin unit; an ethylenically unsaturated monocarboxylic acid unit other than (meth)acrylic acid; and an ethylenically unsaturated dicarboxylic acid (for example, maleic acid, fumaric acid, itaconic acid, and citraconic acid) unit, and anhydride units thereof.
  • a vinyl ester unit for example, a vinyl ether unit; an olefin unit; a substituted olefin unit; an ethylenically unsaturated monocarboxylic acid unit other than (meth)acrylic acid; and an ethylenically unsaturated dicarboxylic acid (for example, maleic acid, fumaric acid, itaconic acid, and citraconic acid) unit, and anhydride units thereof.
  • the rubber polymer a polymer having rubber elasticity may be used.
  • Examples of the rubber polymer may include natural rubber; polybutadiene; polyisoprene; polychloroprene; an ethylene-propylene copolymer; an acrylonitrile-butadiene-based copolymer; and an aromatic vinyl compound-diene-based copolymer.
  • the aromatic vinyl compound-diene-based copolymer means a copolymer containing an aromatic vinyl compound unit and a diene unit.
  • the aromatic vinyl compound unit means a structural unit having a structure obtained by polymerizing an aromatic vinyl compound.
  • the diene unit means a structural unit having a structure obtained by polymerizing a diene.
  • the aromatic vinyl compound unit and the diene unit are not limited by the respective production methods, and may be structural units obtained by any optional production methods.
  • Examples of the aromatic vinyl compound for forming the aromatic vinyl compound unit may include styrene, styrene derivatives (for example, ⁇ -methylstyrene, 2-methylstyrene, 3-methylstyrene, 4-methylstyrene, and 2,4-dimethylstyrene), and vinylnaphthalene (for example, 1-vinylnaphthalene and 2-vinylnaphthalene).
  • styrene for example, ⁇ -methylstyrene, 2-methylstyrene, 3-methylstyrene, 4-methylstyrene, and 2,4-dimethylstyrene
  • vinylnaphthalene for example, 1-vinylnaphthalene and 2-vinylnaphthalene
  • aromatic vinyl compound-diene-based copolymer a copolymer in which the aromatic vinyl compound unit is one or more selected from the group consisting of a styrene unit and a styrene derivative unit is preferable, and a copolymer in which the aromatic vinyl compound unit is a styrene unit is more preferable.
  • Examples of the diene for forming the diene unit may include 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, and 1,3-pentadiene.
  • the diene one type thereof may be solely used, and two or more types thereof may also be used in combination at any ratio.
  • the aromatic vinyl compound-diene-based copolymer a copolymer in which the diene unit is a 1,3-butadiene unit is preferable.
  • the amount of the acrylic polymer in the resin is preferably 50% by weight or more, more preferably 70% by weight or more, and still more preferably 90% by weight or more, and is usually 100% by weight or less, relative to the amount of the resin.
  • the amount of the aromatic vinyl compound-diene-based copolymer in the resin is preferably 50% by weight or more, more preferably 70% by weight or more, and still more preferably 90% by weight or more, and is usually 100% by weight or less, relative to the amount of the resin.
  • the weight-average molecular weight (Mw) of the polymer contained in the resin is preferably 10,000 or more, more preferably 50,000 or more, and still more preferably 80,000 or more, and is preferably 1,000,000 or less, more preferably 800,000 or less, and still more preferably 700,000 or less.
  • the weight-average molecular weight may be determined as a polystyrene equivalent value by gel permeation chromatography (GPC) using tetrahydrofuran (THF) as a mobile phase.
  • the polymer constituting the resin may be produced by any optional method.
  • Examples of the production methods may include, but are not limited to, solution polymerization, suspension polymerization, bulk polymerization, and emulsion polymerization.
  • the metal compound may include a monovalent metal salt and a divalent or higher polyvalent metal salt, and a polyvalent metal salt is preferable.
  • salt as used herein means a compound that is obtainable by the reaction of an acid and a base.
  • Examples of the metal atom constituting the metal compound may include atoms belonging to transition metal elements such as a copper atom, a zinc atom, and an iron atom.
  • Examples of the metal compound that is a polyvalent metal salt and contains a transition metal atom having a valence (II) or more and an organic compound may include a copper compound which is an organic substance (for example, copper(II) dimethyldithiocarbamate, copper(II) ethoxide, copper(II) ethylacetoacetate, copper(II) 2-ethylhexanoate, copper(II) gluconate, copper(II) isobutyrate, copper(II) isopropoxide, copper(II) methacrylate, copper(II) phthalate, copper(II) phthalocyanine, and copper(II) stearate); a tin compound which is an organic substance (for example, tin acetate, tin acetylacetonate, tin ethoxide, tin 2-ethylhexanoate, and tin stearate); an iron compound which is an organic
  • Examples of the metal compound which is a polyvalent metal salt and includes a transition metal atom having a valence (II) or more and an inorganic ion may include a copper compound which is an inorganic substance (for example, copper chromite, copper(II) nitrate, copper(II) sulfate, and copper(II) thiocyanate); a tin compound which is an inorganic substance (for example, tin sulfate); an iron compound which is an inorganic substance (for example, iron diphosphate, iron nitrate, and iron sulfate); and a zinc compound which is an inorganic substance (for example, zinc carbonate, zinc sulfate, and zinc thiocyanate).
  • a copper compound which is an inorganic substance for example, copper chromite, copper(II) nitrate, copper(II) sulfate, and copper(II) thiocyanate
  • one type thereof may be solely contained in the adhesive agent, and two or more types thereof may also be contained in the adhesive agent in combination at any ratio.
  • the metal compound is preferably one or more selected from the group consisting of a copper compound, a zinc compound, and an iron compound, one or more selected from the group consisting of a copper compound and a zinc compound, more preferably a copper compound, and particularly preferably copper(II) sulfate or copper(II) stearate.
  • the metal compound is preferably a zinc compound, more preferably zinc(II) stearate.
  • the metal compound is preferably a compound that does not contain any of a hydroxy group, a hydroxy ion, and water. This configuration can suppress the generation of water by the reaction between hydrogen sulfide and the metal compound.
  • the metal compound does not contain chloride ions.
  • This configuration can suppress the formation of a stable compound by the reaction between the chloride ion and the lithium ion.
  • the weight ratio of the metal compound is usually 1% by weight or more, preferably 10% by weight or more, and more preferably 20% by weight or more, and is usually less than 60% by weight, preferably 50% by weight or less, and more preferably 45% by weight or less, relative to the total weight of the metal compound and the resin contained in the adhesive agent.
  • the adhesive agent can effectively exhibit the ability to absorb hydrogen sulfide.
  • the weight ratio of the metal compound is equal to or less than the above-mentioned upper limit value, the adhesive strength of the adhesive agent can be improved.
  • the adhesive agent of the present embodiment may contain an optional component in addition to the metal compound and the resin.
  • the optional component may include various additives such as a gas adsorbent other than the metal compound (for example, activated carbon), a tackifier, and a softener.
  • a gas adsorbent other than the metal compound for example, activated carbon
  • a tackifier for example, a tackifier
  • a softener for example, a tackifier
  • the proportion of these additives in the adhesive agent may be 0 to 10 parts by weight relative to 100 parts by weight of the resin.
  • the production method of the adhesive agent is not particularly limited, and the adhesive agent may be produced by any method publicly known in prior art.
  • the adhesive agent may be produced by dissolving the resin containing the polymer and other optional components in a solvent, adding a metal compound to the resulting solution, and stirring the mixture to disperse the metal compound.
  • the adhesive agent of the present embodiment is usually used in a battery containing a sulfide-based solid electrolyte.
  • sulfide-based solid electrolyte described herein means a solid electrolyte containing a sulfide.
  • Examples of the solid electrolyte containing a sulfide may include a sulfide material produced using a raw material composition containing Li 2 S and sulfides of elements of Groups 13 to 15 in the Periodic Table.
  • Specific examples of the raw material composition may include a composition containing Li 2 S and P 2 S 5 , a composition containing Li 2 S and SiS 2 , a composition containing Li 2 S and GeS 2 , and a composition containing Li 2 S and Al 2 S 3 .
  • a composition containing Li 2 S and P 2 S 5 is preferable from the viewpoint of excellent lithium-ion conductivity.
  • the raw material composition of the sulfide-based solid electrolyte may contain, in addition to Li 2 S and P 2 S 5 described above, one or more sulfides selected from the group consisting of Al 2 S 3 , B 2 S 3 and SiS 2 to the extent that the ionic conductivity is not reduced. This configuration can stabilize the glass component in the sulfide-based solid electrolyte.
  • the raw material composition of the sulfide-based solid electrolyte may contain, in addition to Li 2 S and P 2 S 5 , one or more types of lithium ortho-oxoate selected from the group consisting of Li 3 PO 4 , Li 4 SiO 4 , Li 4 GeO 4 , Li 3 BO 3 and Li 3 AlO 3 . This configuration can stabilize the glass component in the sulfide-based solid electrolyte.
  • the molar fraction of Li 2 S in the raw material composition of the sulfide-based solid electrolyte is preferably 50% or more, and more preferably 60% or more, and is preferably 74% or less, from the viewpoint that a sulfide-based solid electrolyte having crosslinked sulfur can be more reliably obtained.
  • Examples of the method for producing the sulfide-based solid electrolyte from the above-mentioned raw material compositions may include an amorphization method such as a mechanical milling method and a melt quenching method.
  • the sulfide-based solid electrolyte may be sulfide glass or crystallized sulfide glass.
  • the sulfide glass may be obtained, for example, by the amorphization method described above.
  • the crystallized sulfide glass may be obtained, for example, by heat-treating of the sulfide glass.
  • the sulfide-based solid electrolyte is preferably crystallized sulfide glass represented by Li 7 P 3 S 11 from the viewpoint of exhibiting excellent Li ion conductivity.
  • Examples of the method for producing the crystallized sulfide glass represented by Li 7 P 3 S 11 may include a method in which Li 2 S and P 2 S 5 are mixed at a molar ratio of 70:30 and amorphized by a ball mill to obtain a sulfide glass, and the obtained sulfide glass is heat-treated at 150°C to 360°C.
  • the adhesive agent of the present embodiment is used, for example, in the above-mentioned battery containing the sulfide-based solid electrolyte.
  • the battery containing the sulfide-based solid electrolyte usually includes a positive electrode and a negative electrode, and a layer of the sulfide-based solid electrolyte is disposed as an electrolyte layer between the positive electrode and the negative electrode.
  • the positive electrode usually includes a layer containing a positive electrode active material and a positive electrode current collector.
  • the negative electrode usually includes a layer containing a negative electrode active material and a negative electrode current collector.
  • the battery may be a wound type battery having a structure in which the positive electrode, the solid electrolyte layer, the negative electrode, and the separator are layered and then wound, or a layered type battery having a structure in which a plurality of layered bodies, in each of which the positive electrode, the solid electrolyte layer, the negative electrode, and the separator are layered, are further layered.
  • the outer casing of the battery may be any of a cylindrical casing, a rectangular casing, and a laminate-type casing.
  • the battery containing the sulfide-based solid electrolyte is preferably a lithium-ion all-solid secondary battery in which the electrolyte is the sulfide-based solid electrolyte.
  • the adhesive agent of the present embodiment is used for effecting adhesion of constituent members of the battery containing the sulfide-based solid electrolyte.
  • the adhesive agent of the present embodiment may be used in place of the adhesive agent used in the battery in prior art.
  • the adhesive agent of the present embodiment may be used for effecting adhesion between an outer casing of the battery and an electrode wound body or layered body containing the electrodes and the sulfide-based solid electrolyte, and for adhesion between the outer casing of the battery and a tab that extends from the current collector constituting the electrode.
  • the adhesive agent may also be formed in an adhesive agent layered body for battery and used as described in the section (2. Adhesive layered body for battery).
  • the adhesive agent is preferably used for effecting adhesion of the outer casing and the electrode layered body including the electrodes and the sulfide-based solid electrolyte.
  • the adhesive agent is preferably used for effecting adhesion of the tab and other constituent members.
  • An adhesive layered body for battery according to an embodiment of the present invention includes a substrate and a layer of the adhesive agent for battery provided on the substrate.
  • the adhesive layered body for battery according to the present embodiment includes the layer of the above-mentioned adhesive agent for battery, it has the same advantageous effect as the above-mentioned adhesive agent for battery. That is, the adhesive layered body for battery has the hydrogen sulfide absorption ability and good adhesive strength to an adherend.
  • Fig. 1 is a schematic cross-sectional view of the adhesive layered body for battery according to an embodiment of the present invention.
  • an adhesive layered body for battery 100 includes a substrate 10 and a layer 20 of the adhesive agent for battery provided on the substrate 10 so as to be in contact with one surface 10U of the substrate 10.
  • the adhesive layered body for battery 100 of the present embodiment has only one layer of the adhesive agent for battery.
  • the adhesive layered body for battery may include the substrate and two layers of the adhesive agent for battery, and the layers of the adhesive agent for battery may be provided on the respective surfaces of the substrate.
  • a substrate formed of any optional material may be used.
  • a substrate made of a resin containing a polymer may be used.
  • the resins for forming the substrate may include a polyester (for example, polyethylene terephthalate (PET), polyethylene naphthalate, polybutylene terephthalate, and polybutylene naphthalate); a polyolefin (for example, polyethylene, polypropylene, an ethylene-propylene copolymer); a polyvinyl alcohol; a polyvinylidene chloride; a polyvinyl chloride; a vinyl chloride-vinyl acetate copolymer; a polyvinyl acetate; a polyamide; a polyimide; a cellulose-based resin; a fluororesin; a polyether; a polyetheramide; a polyphenylene sulfide; a polystyrene-based resin (for example, a polystyrene); a polycarbonate; and a polyethersulfone. Two or more types of these may be used in combination.
  • PET polyethylene terephthalate
  • the substrate may have a single-layer structure or a multi-layer structure.
  • the substrate may be the one that has been subjected to a surface treatment such as a chromic acid treatment, an ozone treatment, or a corona treatment.
  • a surface treatment such as a chromic acid treatment, an ozone treatment, or a corona treatment.
  • the thickness of the substrate may be any optional thickness, and for example, is from 1 ⁇ m to 200 ⁇ m, and preferably from 5 ⁇ m to 50 ⁇ m.
  • the substrate may be in the form of a tape
  • the adhesive layered body for battery may be in the form of an adhesive tape
  • the substrate may be produced by an optional method. Alternatively, a commercially available product may be adopted as the substrate.
  • the layer of the adhesive agent for battery is a layer formed from an adhesive agent for battery, and usually includes the above-mentioned adhesive agent for battery.
  • the layer of the adhesive agent for battery contains a metal compound and a resin, and the metal compound is contained in an amount of 1% by weight or more and less than 60% by weight relative to the total weight of the metal compound and the resin.
  • the layer of the adhesive agent for battery may be formed in any optional method.
  • the layer of the adhesive agent for battery may be formed by applying, on a substrate, the adhesive agent for battery as it is or diluted with a solvent to form a coating film, and drying the coating film if necessary.
  • the layer of the adhesive agent for battery may be formed by applying the adhesive agent for battery or a diluted liquid thereof on a release film to form a layer of the adhesive agent for battery, and transferring the layer onto a substrate.
  • any optional method may be employed, and the coating may be performed by a coating method using any optional coater such as a gravure roll coater, a reverse roll coater, a kiss roll coater, a dip roll coater, a bar coater, a knife coater, a spray coater, a comma coater, a direct coater, and a die coater.
  • any optional coater such as a gravure roll coater, a reverse roll coater, a kiss roll coater, a dip roll coater, a bar coater, a knife coater, a spray coater, a comma coater, a direct coater, and a die coater.
  • the layer of the adhesive agent for battery may be formed by melt-coextruding a substrate and the adhesive agent to be in a form of a film.
  • the layer of the adhesive agent for battery may have any optional thickness, for example, 2 ⁇ m to 100 ⁇ m, preferably 5 ⁇ m to 20 ⁇ m.
  • the adhesive layered body for battery has the hydrogen sulfide absorption ability and good adhesive strength to an adherend.
  • the adhesive layered body for battery has the peel strength, measured using a copper plate as the adherend according to JIS Z0237, of preferably 40 N/m or more, more preferably 50 N/m or more.
  • the adhesive layered body for battery is usually used in the battery containing the sulfide-based solid electrolyte.
  • the adhesive layered body for battery may be used for effecting adhesion of the constituent members of the battery.
  • Specific examples of such a use method of the adhesive layered body for battery may include a use application of causing adhesion of the adhesive layered body for battery to the periphery of the electrode layered body including the electrodes and the solid electrolyte, thereby putting the constituent elements of the electrode layered body together, and a use application of causing adhesion of the adhesive layered body for battery to the periphery of the tab that extends from the current collector.
  • the weight-average molecular weight of the polymer was measured by GPC using THF as a mobile phase.
  • Polystyrene was used as a reference material.
  • the adhesive layered bodies obtained in Examples and Comparative Examples were brought into contact with an argon gas containing 10 ppm (weight basis) of hydrogen sulfide for 10 minutes. Subsequently, it was confirmed by visual observation whether or not the layers of the adhesive agent provided in the adhesive layered bodies were discolored.
  • the adhesive layered body had the ability to absorb hydrogen sulfide.
  • the layer of the adhesive agent was not discolored, it was determined that the adhesive layered body did not have the ability to absorb hydrogen sulfide.
  • the peel strength was measured by the 90° peel method according to JIS Z0237 "adhesive tape/adhesive sheet test method".
  • Adhesion of the surface of the adhesive layered body on the side of the adhesive layer to a copper plate was effected, and a manual pressing device (2.0 kg roller) was reciprocated twice to prepare a sample for evaluation.
  • High peel strength is indicative of strong adhesive strength of the adhesive agent and the adhesive layered body.
  • a binder solution was produced by the following procedure.
  • aqueous dispersion liquid was adjusted to a pH of 7 using a 10wt% NaOH aqueous solution. Furthermore, a heat treatment under reduced pressure was performed to remove unreacted monomers.
  • aqueous dispersion liquid of the binder polymer adjusted to a solid content concentration of 43% by weight, 500 g of xylene was added, and the water was evaporated under reduced pressure. With this operation, the solvent of the binder polymer was replaced from water to the organic solvent, so that a binder solution with a water content of 28 ppm (weight basis) was obtained.
  • xylene was added as an organic solvent in an amount by which the solid content concentration of the mixture was adjusted to 65% by weight. Subsequently, the mixture was mixed with a planetary mixer to prepare a slurry composition for solid electrolyte layer having the solid content concentration of 65% by weight.
  • the obtained slurry composition was applied onto a copper foil with a thickness of 12 ⁇ m using a doctor blade with a gap of 100 ⁇ m. Then, the resulting foil was dried on a hot plate at 50°C for 20 minutes to form a coating film composed of the solid electrolyte on the copper foil. The coating film thus formed was scraped off from the copper foil except for a 40 mm square part, leaving the coating film formed in a square shape with each edge of 40 mm on the copper foil.
  • a copper foil was overlaid on the coating film so as to sandwich the remaining square-shaped coating film, followed by pressing with a press pressure of 20 MPa. After pressing, the resulting product was processed into a shape having the square-shaped part with each edge of 40 mm and two tape-like tabs. Each of the two tabs is provided so as to extend from the center of each of the two opposing edges of the square-shaped part. As a result, a cell having a structure in which the solid electrolyte coating film formed in the square shape with each edge of 40 mm was sandwiched between the two copper foils with each edge of 40 mm was obtained.
  • the periphery of the square-shaped part of the cell except for the tabs was wrapped with the adhesive layered body. Subsequently, the square-shaped part was sealed with an aluminum laminate film over the adhesive layered body to obtain a test cell.
  • Resistance value increase rate % R1 ⁇ R0 / R0 ⁇ 100
  • Small value of increase rate from the initial resistance value is indicative of protection of the test cell by the adhesive layered body.
  • the increase rate from the initial resistance value is an index indicating that hydrogen sulfide is absorbed by the adhesive layered body and deterioration of the battery is prevented in the battery containing the sulfide-based solid electrolyte.
  • a 2 L glass container equipped with a stirrer and a condenser was charged with 400 g of toluene, 85 g of 2-ethylhexyl acrylate, and 15 g of butyl acrylate, and the mixture was mixed and heated under reflux.
  • an initiator solution prepared by dissolving 0.1 g of dicumyl peroxide in 5 g of toluene was added to initiate polymerization.
  • the reaction liquid was cooled and poured into methanol.
  • the polymer was then collected by filtration.
  • an acrylic acid ester copolymer weight-average molecular weight (Mw) of 150,000
  • the copolymer shown in Table 1 (the copolymer produced in Production Example 1 or Production Example 2) was dissolved in xylene so that the concentration of the copolymer was 10% by weight.
  • the metal compound (zinc stearate or copper sulfate) shown in Table 1 was added to this and dispersed.
  • the amount of the metal compound to be added was determined such that the weight of the metal compound was adjusted to the weight percentage shown in Table 1 relative to the total weight of the polymer and the metal compound in the dispersion liquid.
  • a dispersion liquid as an adhesive agent was obtained.
  • the obtained dispersion liquid was applied onto a polyethylene terephthalate (PET) film with a thickness of 50 ⁇ m as a substrate to obtain a coating film.
  • the coating film was dried by heating on a hot plate at 60°C for 20 minutes to obtain an adhesive layered body having a layer configuration of (PET film) / (layer of adhesive agent).
  • the thickness of the layer of the adhesive agent was 20 ⁇ m
  • the copolymer shown in Table 1 was dissolved in xylene so that the concentration of the copolymer was 10% by weight to obtain an adhesive agent.
  • the obtained adhesive agent was applied onto a PET film with a thickness of 50 ⁇ m to obtain a coating film.
  • the coating film was dried by heating on a hot plate at 60°C for 20 minutes to obtain an adhesive layered body having a layer configuration of (PET film) / (layer of adhesive agent).
  • the thickness of the layer of the adhesive agent was 20 ⁇ m.
  • the “adhesive composition” indicates the weight percentage of each component relative to the total weight of the metal compound and the resin.
  • the adhesive layered bodies of Examples 1 to 4 in which the amount of the metal compound is 1% by weight or more and less than 60% by weight relative to the total weight of the polymer and the resin, have an ability to absorb hydrogen sulfide, have good peel strength values, and have low resistance value increase rates.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Electrochemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Composite Materials (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Battery Electrode And Active Subsutance (AREA)
EP21849441.7A 2020-07-28 2021-07-09 Adhesive for battery, and adhesive layered body for battery Pending EP4191762A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2020127619 2020-07-28
PCT/JP2021/025915 WO2022024717A1 (ja) 2020-07-28 2021-07-09 電池用接着剤及び電池用接着積層体

Publications (1)

Publication Number Publication Date
EP4191762A1 true EP4191762A1 (en) 2023-06-07

Family

ID=80036301

Family Applications (1)

Application Number Title Priority Date Filing Date
EP21849441.7A Pending EP4191762A1 (en) 2020-07-28 2021-07-09 Adhesive for battery, and adhesive layered body for battery

Country Status (6)

Country Link
US (1) US20230272248A1 (ja)
EP (1) EP4191762A1 (ja)
JP (1) JPWO2022024717A1 (ja)
KR (1) KR20230047077A (ja)
CN (1) CN115803943A (ja)
WO (1) WO2022024717A1 (ja)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024080339A1 (ja) * 2022-10-12 2024-04-18 大日本印刷株式会社 全固体電池

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013149603A (ja) 2011-12-20 2013-08-01 Nitto Denko Corp 電池用粘着テープ、及び該粘着テープを使用した電池
JP6164900B2 (ja) * 2013-04-05 2017-07-19 共同印刷株式会社 硫黄系ガス吸着用樹脂組成物
KR20190131499A (ko) 2017-03-27 2019-11-26 니폰 제온 가부시키가이샤 전극 구성체 고정용 접착제 및 전기 화학 소자
JP2020082624A (ja) * 2018-11-29 2020-06-04 共同印刷株式会社 ガス吸収フィルム
JP7405507B2 (ja) * 2019-01-09 2023-12-26 イビデン株式会社 硫黄系ガス吸着構造体及び組電池

Also Published As

Publication number Publication date
US20230272248A1 (en) 2023-08-31
CN115803943A (zh) 2023-03-14
WO2022024717A1 (ja) 2022-02-03
KR20230047077A (ko) 2023-04-06
JPWO2022024717A1 (ja) 2022-02-03

Similar Documents

Publication Publication Date Title
EP3276734B1 (en) All-solid secondary battery
CN102746801B (zh) 电化学装置用粘合带
EP2903064B1 (en) Electroconductive adhesive composition for electrochemical device electrode, current collector with adhesive layer, and electrode for electrochemical device
EP1629556B1 (en) Composite binder for an electrode with dispersants chemically bound
CN104159987B (zh) 粘合带
CN115050922B (zh) 一种水性粘结剂及其制备方法和应用
EP3734695A1 (en) Composition for nonaqueous secondary battery functional layers, battery member for nonaqueous secondary batteries, method for producing laminate for nonaqueous secondary batteries, and nonaqueous secondary battery
CN106848160A (zh) 多孔层
EP3506394B1 (en) Composition for nonaqueous secondary battery functional layers, functional layer for nonaqueous secondary batteries, nonaqueous secondary battery, and method for producing electrode for nonaqueous secondary batteries
EP3474348B1 (en) Composition for non-aqueous secondary battery function layer, functional layer for non-aqueous secondary battery, and non-aqueous secondary battery
US9947929B2 (en) Binder composition for nonaqueous battery electrodes, slurry for nonaqueous battery electrodes, nonaqueous battery electrode, and nonaqueous battery
EP3486981B1 (en) Binder composition for solid electrolyte batteries
EP3223347B1 (en) Binder composition for lithium-ion secondary battery electrode
EP3512013B1 (en) Binder composition for all-solid-state battery, slurry composition for all-solid-state battery, electrode for all-solid-state battery, and all-solid-state battery
WO2015012366A1 (ja) 電極用バインダー、電極用組成物及び電極シート
US11557766B2 (en) Binder composition for all-solid-state secondary battery, slurry composition for all-solid-state secondary battery, functional layer for all-solid-state secondary battery, and all-solid-state secondary battery
EP4191762A1 (en) Adhesive for battery, and adhesive layered body for battery
EP3904406B1 (en) Binder composition for all-solid-state secondary batteries
EP3734697A1 (en) Composition for nonaqueous secondary battery functional layers, battery member for nonaqueous secondary batteries, method for producing laminate for nonaqueous secondary batteries, and nonaqueous secondary battery
JP2013164972A (ja) 二次電池電極バインダ用重合体とその製造方法、二次電池用電極、およびリチウムイオン二次電池
WO2023008151A1 (ja) 全固体二次電池用スラリー組成物、固体電解質含有層及び全固体二次電池
US20230327183A1 (en) Method of producing binder composition for all-solid-state secondary battery, method of producing slurry composition for all-solid-state secondary battery, method of producing solid electrolyte-containing layer, and method of producing all-solid-state secondary battery
US20230033554A1 (en) Binder composition for secondary battery, slurry composition for secondary battery, solid electrolyte-containing layer, all-solid-state secondary battery, and method of producing all-solid-state secondary battery
US20230261255A1 (en) Slurry composition for all-solid-state secondary battery, solid electrolyte-containing layer, and all-solid-state secondary battery
WO2022249933A1 (ja) 全固体二次電池用バインダー組成物、全固体二次電池用スラリー組成物、全固体二次電池用機能層、および全固体二次電池

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20230118

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)